Abstract
Although focused interests are often associated with a diagnosis of autism, they are common in nonautistic individuals as well. Previous studies have explored how these interests impact cognitive, social, and language development. While some research has indicated that they are advantageous, other results (particularly those focused on autistic children) have suggested that strong interests can detract from learning. In this pre-registered study, we asked whether focused interests support word learning in 44 autistic children and a vocabulary-matched sample of 44 nonautistic children (mean ages 58 and 34 months respectively). In a word-learning task administered over Zoom, children were exposed to an action labeled by a novel word. The action was either depicted by their focused interest or by a neutral image; stimuli were personalized for each child. At test, they were asked to identify the referent of the novel word, and their eye gaze was evaluated as a measure of learning. The preregistered analyses revealed an effect of focused interests, and post-hoc analyses clarified that autistic children learned the novel word in both the focused interest and neutral conditions, while nonautistic children only showed evidence of learning in the neutral condition. These results suggest that focused interests are not disruptive for vocabulary learning in autism, and thus they could be utilized in programming that supports early language learning in this population.
Keywords: autism, language, word learning, interests, verbs
LAY SUMMARY
Although focused interests are often associated with a diagnosis of autism, they are common in nonautistic individuals as well. Previous studies have explored how these interests impact cognitive, social, and language development. While some research has indicated that can support learning, other results (particularly those focused on autistic children) have suggested that strong interests can impede learning. In this study, we asked whether focused interests support word learning in 44 autistic children and 44 nonautistic children with similar language skills (average ages 58 and 34 months respectively). In an online task, children were taught a new word for an action. The action was either demonstrated by their focused interest or by a neutral image. At test, they were asked to identify the meaning of the new word. Results indicated that autistic children learned the word in both the focused interest and neutral conditions, while nonautistic children only learned in the neutral condition. These results suggest that focused interests could be utilized for supporting early language learning in children on the autism spectrum.
Young children often show focused interests (e.g., dinosaurs, birds, Pokémon), which can be considered “fascinations with particular categories of objects or activities”, wherein children may “display a passionate, sometimes bordering on obsessive, attraction to items in their interest category” (DeLoache et al., 2007, p. 1579). Focused interests have been observed in girls and boys (Alexander et al., 2008) and are reported in 30% to 50% of preschool children (DeLoache et al, 2007; Alexander et al. 2008). Strong interests have a number of advantages for learning, including increased knowledge, attention, recognition, and recall (Hidi, 1990; Renninger, 1992; Renninger & Wozniak, 1985; Alexander et al., 2008). Previous findings have also suggested that strong interests are positively associated with nonverbal cognition and language abilities (Alexander et al., 2002; Johnson et al., 2004; Johnson & Eilers, 1998). Some researchers have additionally considered the value of strong interests for language learning in young children: children’s interest in an area predicts word knowledge (Mani & Ackermann, 2018) and performance in a word-learning task (Ackermann, Hepach, & Mani, 2020; Ackermann et al., 2023). Ackermann and colleagues (2020) taught 30-month-olds new nouns for objects in four different categories (animals, clothes, vehicles, drinks); for each category, they obtained parent ratings on whether it was of high or low child interest. Nouns in high-interest categories were learned better than nouns in low-interest categories, and the researchers concluded that personal interest may scaffold language learning. These results are broadly consistent with other word-learning studies in even younger 24-month-old children, indicating that higher levels of existing word knowledge in a category facilitates learning new words in that same semantic category (Borovsky et al., 2016).
The implications of focused interests for learning have also been extensively considered in the development of individuals on the autism spectrum. “Restricted and repetitive interests” are included as one of the diagnostic features of Autism Spectrum Disorder (APA, 2013), and strong interests are experienced by the vast majority of autistic individuals (Klin et al., 2007; Grove et al., 2018; Nowell et al., 2021; Spiker et al., 2011). Although the intensity of interests may be stronger in autistic individuals than in people who do not have autism (Anthony et al., 2013; Burrows et al., 2021; Larose et al., 2021), the number and topic of interests may be similar (Anthony et al., 2013), including television, animals, construction, and art (Nowell et al., 2021).
There remains considerable debate over whether these interests are disruptive versus adaptive for cognitive, social, and daily functioning in individuals on the autism spectrum. Strong interests are seen by some caregivers and professionals as interfering (Anthony et al. 2013; Nowell et al., 2021) and requiring treatment (e.g., Carter et al. 2020). Indeed, some research has suggested that strong interests can distract individuals from attending to information in the environment. In a gaze-tracking study, Sasson and Touchstone (2013) reported that autistic preschoolers prioritized attention to images representing strong interests over attention to faces; the nonautistic sample did not show this pattern. Other research has suggested that depictions of strong interests can also distract nonautistic children from social information (Sasson et al., 2011; Ambarchi et al., 2022; we note that previous literature has often referred to these study samples as “typically developing”, although here we are choosing to use the term “nonautistic” in order to avoid ableist language; Bottema-Beutel et al., 2021). It is noteworthy, though, that these studies have pitted attention to social cues against focused interests, rather than harnessing focused interests to scaffold attention. Accordingly, strength-based approaches view these interests as tools for learning. Patten Koenig and Hough Williams (2017) interviewed adults on the autism spectrum and learned that focused interests were experienced as strengths that helped (rather than hindered) daily functioning and played an important role in managing anxiety. Many of the adults were engaged in vocational and avocational pursuits surrounding their focused interests (see also Chiodo et al., 2017).
The question of whether focused interests can scaffold learning for autistic individuals has received the most attention for social communication skills. Consensus generally affirms that focused interests can effectively be harnessed to support social communication (e.g., Boyd, Conroy, Mancil, Nakao, & Alter, 2007; Dunst & Hamby, 2016; Gunn & Delafield-Butt, 2016; Harrop et al., 2019; Ninci et al., 2019; Sivaraman & Fahmie, 2018). Similarly, there is evidence of positive collateral effects on self-image, mood, and attention (Winter-Messiers, 2007; Vismara & Lyons, 2007). Moreover, some research has also focused on a potential link between strong interests and language skills for young autistic children. For instance, Jacques and colleagues (2018) found that children on the autism spectrum were more inclined than their nonautistic peers to show strong interests in language- and literacy-related objects or activities (e.g., picture dictionary, books, magnetic letters); in other work, similar strong interests were found to facilitate communication and language skills in hyperlexic autistic children (Osterlenk et al., 2023). Larose and colleagues (2021)—in their development of a parent survey capturing the strengths and interests of autistic preschoolers—also reported that, for young autistic children, strong interests were perceived by parents to support language and literacy development. In a recent study of interests and word learning in a small sample of school-age autistic individuals, Rothwell and colleagues (2023) found that words reported to be in a high interest category (i.e., animals) were retained better than those of low interest (i.e., objects) but only for 5-minute retention tests; apparent memory consolidation for the object category meant that the condition effect had diminished by 24 hours later.
There are several reasons why this link between strong interests and language skills is a particularly notable connection. First, autistic children often experience language delays (e.g., Nitzan et al., 2022; Tager-Flusberg, 2016), reduced vocabulary size, and slowed progression of morphology and grammar (e.g., Charman et al., 2003; Luyster et al., 2007; Pickles et al., 2014). As autistic children age, there is wide variability in language outcomes, with a substantial minority of individuals remaining nonspeaking through adulthood (Tager-Flusberg & Kasari, 2013; Pickles et al., 2014). Early language development predicts language outcomes, and the most substantial language gains seem to happen before the age of 8–10 years (Pickles et al., 2014; Bal et al., 2018). Therefore, identifying strategies to support foundational language skills is a priority; focused interests may offer a potential strategy for scaffolding this essential domain.
Here, we aim to more directly address the question of whether invoking a child’s focused interest results in more robust language learning, specifically, word learning, than invoking “neutral” items for children on the autism spectrum, as well as their nonautistic peers. Unlike research on how children learn about the interests themselves (e.g., Ackermann et al., 2020), the current study presents word meanings that are unrelated to the interest; the interests are used only to depict a novel action. Importantly, this allows us to explore how interests could be leveraged to promote generalized learning (i.e., not just about concepts that are related to the interest). For this reason, we used novel verbs as the target words to be learned, which could be depicted using an object that invoked the child’s interest. Using a quasi-experimental design, in which preschool-aged children were taught a new verb for an action, we recorded child gaze to measure their learning of the new verb; novel verb learning studies have been successfully used with autistic children in this age group (e.g., Horvath et al., 2018; Naigles et al., 2011). In contrast to studies that assign neutral and high-interest stimuli universally to all children (e.g., Rothwell, Westermann, & Hartley, 2023; Sasson, Elison, Turner-Brown, Dichter, & Bodfish, 2011), we personalized the stimuli to reflect each child’s own preferences. In accordance with the emerging evidence supporting focused interests as potential learning tools, we hypothesized that children in both groups would look more to the target when it was taught using their focused interest than when it was taught using a neutral item.
METHODS
Participants
Participants were recruited via laboratory databases, internet/social media, word-of-mouth and the SPARK autism research registry (Feliciano et al., 2018). A screening questionnaire was used to determine eligibility based on parent report. Inclusion criteria for all participants were: birth at ≥37 weeks gestation; hears English more than 70% of the time; normal/corrected-to-normal vision; normal hearing; has access to computer/tablet with Zoom software and a stable internet connection.
Additional inclusion criteria for the autism group included a Social Communication Questionnaire (SCQ; Rutter, Bailey & Lord, 2003) total score of equal to or greater than 12 (although the standard cutoff for the SCQ is 15 for children ≥4 years and 12 for children below this age, see Corsello et al., 2007, we applied the lower cutoff to all children), a current medical/educational diagnosis of ASD, and a chronological age of 36–71 months.
Additional inclusion criteria for the nonautistic group included a SCQ score less than 12 and a chronological age of 24–59 months (younger children were targeted to facilitate matching on language ability, because most young autistic children have language delays). Nonautistic participants were excluded if they had a diagnosis of ASD, Language Impairment, Intellectual Disability, or a genetic disorder, or if any family members were diagnosed with ASD. In this way, our use of the term “nonautistic” for the comparison sample is meant to denote that these children did not experience autism nor any of the listed conditions, which commonly co-occur with autism.
Based on the above inclusion/exclusion criteria for participation in the study, the initial sample who completed the study consisted of 125 children. However, after participation in the study, some children were excluded from analyses. In order to be included in the final analysis sample, participants in the autism group required diagnostic confirmation by our study psychologist (more information below in Procedure). Five children in the autism group did not receive diagnostic confirmation based on the DSM-5 criteria (for instance, because they showed reciprocity and nonverbal communication typical for nonautistic children of their age) and were excluded from analyses.
Seven trials from 7 autistic participants and 5 trials from 5 nonautistic participants were then excluded because parent report on the day of the study did not indicate the appropriate level of child focused interest in the images used for the experimental trials (see below). Next, trials were excluded for track loss (see below): 8 trials from autistic children and 2 trials from nonautistic children, as well as both trials from one nonautistic child who was excluded entirely from analysis.1 This process left an interim sample of 60 autistic and 59 nonautistic children. However, preliminary analyses revealed that these two groups (autistic and nonautistic) differed significantly in spoken language ability as measured by expressive vocabulary on the MacArthur Bates Communicative Development Inventory 3, or MCDI3 (Fenson et al., 2006; autistic MCDI3 range 0–100, mean 46 words; nonautistic MCDI3 range 4–100, mean 71 words; t(117) = 4.096, p < .0001). Therefore, to ensure that our final groups did not significantly differ in vocabulary, which was stipulated in our preregistration, we used a bootstrap process with the bootmatch package (Mahr, 2023) in R, requiring a match within +/− 10 spoken words on the MCDI3.
This matching process resulted in a final sample of 44 children per group from 27 US states (autistic group: 35 boys, 9 girls; nonautistic group: 32 boys, 12 girls); the groups did not significantly differ in MCDI3 score (t(86) = 0.44, p = 0.66). The effect size (Cohen’s d) for the difference between the matched groups on MCDI3 was 0.093, and the variance ratio was 0.93; following suggestions in Kover and Atwood (2013), we took these to be acceptably matched. Diagnostic groups differed significantly in age, as is common when groups are matched on language (autistic group: mean age 58 months (range = 40–70 months, SD = 8 months): nonautistic group: mean age 34 months (range = 24–60 months, SD = 9 months), t(86) = 12.6, p < 0.0001). See Table 1 for final sample information.2
Table 1.
Sample Information
| Autistic (n=44) | Nonautistic (n=44) | |
|---|---|---|
|
| ||
| Age range in months | 40–70 | 24–60 |
| Mean age in months (SD) | 58 (8) | 34 (9) |
| MCDI3 score range | 0–100 | 4–100 |
| Mean MCDI3: number of words spoken (SD) | 62 (31) | 65 (29) |
| MCDI3 # children combining words1: | ||
| Not yet | 1 | -- |
| Sometimes | 10 | 3 |
| Often | 30 | 41 |
| Mean Vineland Communication Domain Raw Score (SD) | 25.50 (12.34) | 27.61 (12.93) |
| Mean SCQ Score (SD) | 19.26 (5.12) | 5.20 (2.61) |
| Min-Max SCQ Score | 13–33 | 0–11 |
| Mean Interest in “focused interest” (SD)2 | 3.86 (.46) | 3.95 (.21) |
| Mean Interest in “neutral interest” (SD)2 | 2.18 (.81) | 2.18 (.87) |
| Race | ||
| Asian | 1 | 3 |
| Black | 1 | 0 |
| Hispanic White | 5 | 2 |
| Non Hispanic White | 27 | 34 |
| Hispanic or Non Hispanic Other | 7 | 5 |
MCDI3=MacArthur Bates Communicative Development Inventory 3 (Fenson et al., 2006)
Vineland=Vineland Adaptive Behavior Scale 3rd Ed Parent/Caregiver Form (Sparrow et al., 2016)
SCQ=Social Communication Questionnaire (Rutter, Bailey & Lord, 2003)
Data missing for 3 participants in autistic group.
Per caregiver endorsement of the following statement: “My child is really interested in the above character/object” on a rating scale of 1=Never; 2=Rarely; 3=Sometimes; 4=Often.
Procedure
Procedures and analyses were pre-registered (https://osf.io/ra4un/). Study activities were approved by an Institutional Review Board. This was a remote study. All parent-report measures were collected via REDCap (Harris et al., 2009; 2019) and all “in person” portions were conducted and recorded via Zoom. A screening questionnaire determined eligibility for the study (described above) and additionally asked caregivers to identify and rank their child’s three favorite interests (including toys/characters/topics; e.g., squirrels, Mickey Mouse, guitar). Caregivers whose children were eligible based on the criteria listed above were emailed the links to the electronic consent forms to review independently. A Zoom consent session was scheduled at the caregiver’s convenience, and consent was then discussed via Zoom with the caregiver and any outstanding questions were answered. The caregiver was then asked to sign the consent forms electronically. After consent was complete, the experimenter and caregiver worked together in real time over Zoom to identify the best visual representation of the child’s focused interest using Google Images.3 The caregiver was also presented with images of other participants’ focused interests to identify images that would be “neutral” for their child (i.e., an item that was familiar but towards which the child had no strong feelings). We aimed to reuse focused interest images as another participant’s neutral image, but this was not always possible because we had to ensure that neutral images were truly neutral for a participant (and not unfamiliar or strongly preferred); 83% of focused interest images were able to be reused as another participant’s neutral image. Focused and neutral interest images were paired for each participant based on animacy and size. If a participant had the same focused interest as another participant, a different image depicting the interest was used.
Families were then scheduled for an online study visit. In advance of the study visit, parents were asked to complete questionnaires about their child, including the MCDI3 (Fenson et al., 2006) and the Vineland Adaptive Behavior Scales 3rd Edition Parent/Caregiver form (Sparrow et al., 2016). In advance of the study visit, participants were assigned to one of four condition sets, which counterbalanced assignment of focused versus neutral interest to novel verb (i.e., kibbing/doking) and trial order (focused interest presented in first or second trial). During the study visit, which was conducted on Zoom, the child sat in front of a computer or tablet screen to view the study videos. The child’s gaze was recorded using Zoom during the study session. The experimenters asked the caregiver to ensure that the child was seated centrally in front of the screen and not to speak to the child during the videos.
Finally, although interests were collaboratively identified during the introductory informed consent call with the parents, we asked parents to confirm their child’s interest on the day of data collection in order to measure whether a child’s interest level had changed in the interim period. Therefore, at the end of the experimental session, caregivers were asked to attest to their child’s level of interest in the images (focused interest and neutral) used during the study session on a scale of 1 (never) to 4 (often) for the following statement: My child is really interested in the above character/object. In order to be included in analysis, we required that, on the day of data collection, parents endorse that statement with a rating of “often” for the interest condition and a rating of “never”, “rarely”, or “sometimes” for the neutral condition. Caregivers were also asked to confirm that their child had not developed an aversion to either image in the past week. See Supplementary Materials Table A for the items used for each participant’s focused and neutral interest condition.
Materials
During the remote, Zoom-based study visit, children participated in two verb-learning trials, one per condition, each including a training video and a test video (see Figure 1), without a pause between them. (Many verb learning studies teach only one novel verb per condition, e.g., Dautriche et al., 2014; He & Lidz, 2017; Ma, Juo, Golinkoff, & Hirsh-Pasek, 2023; Yuan & Fisher, 2009) Videos were structured identically for each child, but the images that appeared in them were individualized. Each training video was 24 seconds and presented an object/character completing an action. For one video, the object/character depicted the child’s focused interest, which had been previously determined via caregiver report (as described above). In the other video, the object/character was of neutral interest to the child. Images had a clear background and were cropped to ~300×300 pixels.
Figure 1.

Schematic depiction of stimuli on one trial.
Both training videos began with a Character Introduction phase, which presented the object/character as a still image in center screen, with a pre-recorded voiceover: “Wow, look at my friend! He/she/it is going to play a game with us today!” Then, in the Novel Word Introduction phase the object/character moved in a particular way 4 times; the narrator labeled the action using a novel word each time. The two actions were: (1) spinning, labeled “doking” (/dokɪŋ/); and (2) arcing, labeled “kibbing” (/kɪbɪŋ/). For instance, for objects spinning during the video, the narrator said, “Cool, he/she/it is doking! Ooh, he/she/it is doking. Wow, he/she/it is doking! How fun, he/she/it is doking!” Videos portraying an arcing motion were similarly described but using the word “kibbing.” The phonological forms of the novel words were chosen because they are commonly used in novel verb learning studies (e.g., He & Lidz, 2017; Johnson & de Villiers, 2009) and were not being used in any other verb learning studies in the lab that these same children might also participate in. Audio was recorded by a female speaker of North American English in a child-directed register. Narrations used the most commonly associated gender pronoun for the object/character (“he”, “she” or “it”).
Immediately after each training video, a split-screen test video presented the object/character previously completing the doking/kibbing motion on one side of the screen; the other side depicted the same object/character completing a different motion not previously shown. First, during the Baseline phase (6 sec), children viewed the two scenes side-by-side in silence. Then during the Query phase (2.5 sec), the two scenes disappeared and were replaced with a centrally positioned spiral image serving as a central fixation, and children were asked, “where’s doking/kibbing?” Then, during the Response phase (6 sec), the two scenes reappeared in their original positions and children heard, “Find doking/kibbing.” The assignment of the target/distractor action to the left or right side of the screen was counterbalanced across participants and trials.
Post-Visit Confirmation, Coding and Analysis
After the study visit, diagnostic confirmation and gaze coding were completed by study staff. The process for diagnostic confirmation (our autistic sample was recruited on the basis of having of an existing ASD diagnosis) was based on “best practice” recommendations that autism assessment include developmental/language measures, parent report, direct observation of the child and DSM-5 criteria (e.g., Brian et al., 2019; Zwaigenbaum & Penner, 2018). Therefore, a licensed psychologist with advanced expertise in autism reviewed all available study information, including parent report instruments (e.g., SCQ, MCDI3, Vineland) and the recorded study session; based on this information, she completed a DSM-5 checklist attesting to diagnostic confirmation.
For gaze, three coders viewed the Zoom recordings and manually coded children’s eye gaze during the test videos frame-by-frame at 30 frames/second in Adobe Premiere Pro software.4 Coders were trained on practice videos until they achieved 95% agreement with the training standard, after which they coded independently. All coders were naive to the child’s diagnostic status, what the child was seeing on screen, and which side displayed the target action. Coders indicated whether the child was looking “right”, “left”, “elsewhere” (away from screen but child’s eyes are still visible), or “track loss” (child’s direction of gaze is not visible, e.g., blinking, head turned). Although because this was an at-home study, participants’ screen sizes and children’s distance from the screen varied, we created the videos to have a large space between the “left” and “right” scenes to assist coders in distinguishing them. Inter-coder reliability on whether coders matched on their use of the four direction codes for each frame was calculated for 10% of the videos (based on previous literature; e.g., Naigles et al., 2012; Abu-Zhaya et al., 2023; Delle Luche et al., 2015), each of which were coded by two coders, using the irr package v0.84.1 in R (Gamer & Lemon, 2019). Percent agreement for coder pairs for the autistic group ranged from 92–98% and Cohen’s kappa from 0.89–0.95; for the nonautistic group, percent agreement ranged from 97–99% and Cohen’s kappa from 0.91–0.99.
Following similar studies (e.g., Arunachalam & Dennis, 2019; Horvath et al., 2018), we planned to analyze children’s eye gaze from 1 to 2.5 seconds of the Response phase, which was after children had heard the test query during the Query phase, and immediately at the offset of the second prompt to find the target during the Response phase. This window is appropriate because in similar studies it takes approximately 1 second for children to settle on a scene after a central fixation, and after approximately 2.5 seconds, children tend to shift gaze to the scene they had not previously been fixating. We binned the data into 100 ms bins (approximately 3 frames per bin) and empirical-logit transformed the proportion of looking to the target in each bin. This transformed data served as the dependent variable (Barr, 2008).
RESULTS
As noted above, before creating the final matched sample for analysis, we excluded trials for track loss. Specifically, we excluded trials on which 50% or more of the 6-second Response phase consisted of track loss, indicating that children were inattentive after the test query (50% is a widely-used criterion in developmental studies with autistic and nonautistic children, e.g., Blomquist, Newman, Huang, & Edwards, 2021; Hahn, Snedeker, & Rabagliati, 2015; Horvath et al., 2018; Verdine et al., 2017). Within included trials, individual track loss data points were excluded from analysis. However, data points were included if gaze was directed to neither the target nor distractor (e.g., looking off screen) because our interest was in comparing across conditions rather than comparing to an absolute baseline expectation of looking behavior. This analysis decision differs from some studies using similar paradigms (e.g., Fernald, McRoberts, & Swingley, 2001; Golinkoff, Hirsh-Pasek, Cauley, & Gordon, 1987), which often exclude all looks that are not to either the target or distractor. Notably, research using the related Visual World Paradigm does typically include these data points (see, e.g., Barr, 2008). We think these looks are informative—particularly for autistic children who may have more off-task gaze behavior—and moreover, we included a central fixation before the Response phase, meaning that excluding looks to neither scene would result in missing data as children shifted their gaze from the center to one of the scenes (e.g., Horvath et al., 2018).5 Thus, each data point was a 1 if gaze was to the target, 0 if to the distractor or elsewhere, and removed if the eyes were not visible (i.e., track loss).
Analyses were performed using R Statistical Software (v4.1.2; R Core Team, 2021). Gaze data was formatted using the eyetrackingR package (v0.2.0; Forbes, Dink, & Ferguson, 2021), plots were made using the ggplot2 package (v3.3.5; Wickham, 2016), and statistical tests were done using the lme4 (v1.1–28; Bates et al., 2015), lmerTest (v3.1–3; Kuznetsova, Brockhoff, & Christensen, 2017), and emmeans (v1.7.4–1; Lenth, 2022) packages. The pre-registered analyses are described first, followed by post-hoc analyses. The main effects of interest (e.g., of condition) are reported in the text; parameter estimates for the pre-registered analyses are available in Table 3, and parameter estimates for post-hoc analyses are reported in the Supplementary Materials.
Table 3.
All parameter estimates for the pre-registered analyses.
| Autistic children | ||||
|---|---|---|---|---|
| Parameter | Estimate | SE | t-value | p-value |
| Intercept | 0.43 | 0.22 | 1.99 | .053 |
| Condition | 0.23 | 0.16 | 1.39 | .16 |
| Time | −0.057 | 0.25 | −0.22 | .82 |
| Condition*Time | −0.63 | 0.20 | −3.11 | .0019 |
| Nonautistic children | ||||
| Parameter | Estimate | SE | t-value | p-value |
| Intercept | 0.46 | 0.22 | 2.073 | .045 |
| Condition | −0.98 | 0.17 | −5.66 | <.0001 |
| Time | −0.40 | 0.26 | −1.57 | .12 |
| Condition*Time | 0.52 | 0.21 | 2.48 | .014 |
Pre-registered Analyses
Children’s gaze is depicted in Figure 2 for the autistic group and Figure 3 for the nonautistic group. The x-axis depicts time from 200 ms to 2499 ms of the Response phase; the figure thus includes the period before the analysis window begins (minus the 200 ms that autistic or nonautistic children would be expected to require to shift gaze from the central fixation to one of the scenes, e.g., Chawarksa, Klin & Volkmar, 2003). In the analysis window, children looked at either the target or distractor over 92% of the time in both groups and conditions, with the remaining time spent looking to neither scene (e.g., centrally) or coded as track loss. See Table 2.
Figure 2.

Mean proportion of looking to the target during the Test Phase for the autistic group. The x-axis depicts time from the beginning of the Response period shown in Figure 1, after children have heard the query (e.g., “Where is doking?”); a second iteration of the query (e.g., “Find doking”) began at the onset of this window. Looks to the distractor as well as looks elsewhere are included in the proportion. The analysis window is outlined with a dotted line.
Figure 3.

Mean proportion of looking to the target during the Test Phase for the nonautistic group. The x-axis depicts time from the beginning of the Response period shown in Figure 1, after children have heard the query (e.g., “Where is doking?”); a second iteration of the query (e.g., “Find doking”) began at the onset of this window. Looks to the distractor as well as looks elsewhere are included in the proportion. The analysis window is outlined with a dotted line.
Table 2.
Participants’ mean proportion of looking at the target scene, distractor scene, elsewhere, and track loss during the analysis window of 1–2.5 seconds of the Response phase by group and condition. Standard deviation is in parentheses. Due to rounding, rows do not add up to 1.
| Target | Distractor | Elsewhere | Track loss | |
|---|---|---|---|---|
|
| ||||
| Autistic Group | ||||
| Focused Interest condition | 0.58 (0.32) | 0.39 (0.30) | 0.049 (0.21) | 0.037 (0.16) |
| Neutral condition | 0.61 (0.36) | 0.33 (0.32) | 0.037 (0.20) | 0.022 (0.068) |
|
| ||||
| Nonautistic Group | ||||
| Focused Interest condition | 0.47 (0.35) | 0.50 (0.34) | 0.012 (0.19) | 0.025 (0.11) |
| Neutral condition | 0.64 (0.32) | 0.36 (0.32) | 0.0028 (0.045) | 0.0050 (0.018) |
Per the pre-registered analysis, we asked whether each group showed a difference between conditions in the window from 1–2.5 seconds of the Response phase. For each group, we fit a linear mixed-effects model including a random effect of participant with a random slope for time6 and the following variables as fixed effects: time (in seconds, subtracting 1 because the analysis window began at 1 second), condition (deviation coded with the focused interest condition as 0.5 and the neutral condition as −0.5), and the 2-way interaction between time and condition. A significant interaction between time and condition would indicate that children’s gaze to the target differed by condition as the analysis window unfolded. See Table 3.
For the autism group, the pre-registered analysis yielded no significant simple effect of condition (β = 0.23, t = 1.39, p = .16), indicating no differences between conditions at the beginning of the analysis window, but a significant interaction between time and condition (β = −0.63, t = −3.11, p = .0019). The interaction reflects a difference between conditions in how children’s gaze toward the target unfolded over the course of the analysis window. Post-hoc testing on this interaction using the emtrends function from the emmeans package confirms that the two conditions show significantly different slopes (t = 3.13, p = 0.0020)7; gaze to the target in the focused interest condition decreases over the analysis window, while it increases in the neutral condition. This pattern is likely because children in the focused interest condition had shown an earlier preference for the target, before the pre-selected analysis window began, as evident in Figure 2. A post-hoc (not pre-registered) growth curve analysis (Mirman, 2014) of the portion of the Response phase before the analysis window (from 200–999) ms is reported below in the Post-hoc Analyses section.
For the nonautistic group, the pre-registered analysis yielded a significant simple effect of condition (β = −0.98, t = −5.66, p = <.0001), and a significant interaction between time and condition (β = 0.52, t = 2.48, p = 0.014). The effect of condition indicates that target preference already differed by condition at the beginning of the analysis window (at 1 second), and the interaction reflects a difference between conditions in how gaze toward the target unfolded over the course of the analysis window, as evident in Figure 3. Post-hoc testing on this interaction revealed a significant difference in the slopes (t = −2.48, p = 0.014); children showed a strong preference for the target with a negative slope in the neutral condition, but in the focused interest condition the slope was relatively flat. Here, too, we included a post-hoc growth curve analysis of the portion of the Response phase before the analysis window, from 200–999 ms (see below, in the Post-hoc Analyses section).
Post-hoc Analyses
We also included three sets of additional post-hoc analyses.
Post-hoc Analyses Set #1.
The first post-hoc set of analyses was aimed at answering the question: Could the children’s gaze during the Response phase be driven by the fact that the target scene was the familiar scene, while the distractor scene had not been viewed before? Pilot data (Pelletier & Arunachalam, 2021) suggested that the Baseline phase, during which children saw the two test scenes in silence before being prompted to find the target, would be sufficient to allow children to view and process the novel distractor scene and subsequently have their attention directed by the test query. Nevertheless, it was important to check that this would be the case for the full sample as well. To do so, we examined children’s gaze during the Baseline phase of the Test period. Because the distractor scene was novel, we expected that they might prefer it at the beginning of the Baseline phase, but that they would allocate attention to both scenes by the end of this phase. As Figures 4 and 5 show for the autistic and nonautistic group respectively, even an early preference was not clearly evident; we suspect this is because dynamic action scenes may attract children’s attention differently because of their movement over and above sheer novelty. Whatever the reason, this outcome suggests that their gaze behavior during the Response phase was unlikely to have been driven by the novelty of the distractor scene.
Figure 4.

Mean proportion of looking to the target during the Baseline Phase for the autistic group. Only looks to the target and distractor are included in the proportion.
Figure 5.

Mean proportion of looking to the target during the Baseline Phase for the nonautistic group. Only looks to the target and distractor are included in the proportion.
To further assess gaze during the Baseline phase statistically, we conducted analyses comparing their gaze to the target to “chance” looking over the 6-second Baseline period by removing data points on which children were looking to neither the target nor distractor; this allowed us to test whether children spend more time looking to the target as compared to looking to the distractor. We conducted a series of t-tests within each group and condition separately, with the average proportion of target looking across the 6 seconds serving as the dependent variable. All tests showed that children in both groups were neither significantly above nor below chance at looking to the target during the Baseline phase (autistic focused interest condition: t(38) = 0.82, p = 0.42; autistic neutral condition: t(39) = −0.29, p = .77; nonautistic focused interest condition: t(41) = −0.32, p = 0.75; nonautistic neutral condition: t(39) = 0.92, p = .36). This affirms that children’s gaze behavior during the Response phase was unlikely to have been driven by the pre-existing Baseline preferences for target or distractor.
Post-hoc Analyses Set #2.
The second post-hoc analysis was aimed at further understanding children’s behavior in the Response phase after being asked to identify the target scene. This approach was described as a possible post-hoc analysis in our preregistration: we included data from both groups and added to the previous model predictors of group (with the autistic group coded as 0.5 and the nonautistic group as −0.5) and its interaction with condition, and vocabulary on the MCDI3 (centered around its mean) (along with condition and its interaction with time as in the previous models). We included a group by condition interaction because the main focus of this analysis was to ascertain whether autistic and nonautistic children differ significantly in how they respond to focused interest vs. neutral trials. We included vocabulary because we might expect that children with larger vocabularies would perform better in a language learning task, and it was important to include this individual difference variable when combining children from both groups. The random effects structure was as in the previous models. We found no effect of vocabulary (β = 0.0052, t = 1.59, p = .12) and no effect of group (β = −0.21, t = 1.067, p = .29), but a significant simple effect of condition (β = −0.39, t = −3.21, p = .0014) and a significant 2-way interaction between group and condition (β = 0.41, t = 3.22, p = .0013). The interaction between time and condition was not significant (β = −0.033, t = −0.23, p = 0.82). We pursued the 2-way interaction between group and condition with post-hoc Tukey testing using estimated marginal means; the difference between conditions was significant for the nonautistic group (t = 6.97, p < .0001) but not the autistic group (t = 2.21, p = .12); see Supplementary Tables B–C. Thus, while nonautistic children preferred the target significantly more in the neutral condition than the interest condition, autistic children showed no such disadvantage in the interest condition.
Given these unexpected results, and inspection of Figures 2 and 3 which suggested that nonautistic children may not have learned the novel words in the focused interest condition, we conducted additional analyses to assess whether preference for the target was above chance for each group and condition. As we did for the Baseline period, we removed data points on which children were looking to neither the target nor distractor to test whether children spend more time looking to the target as compared to looking to the distractor, and we conducted a series of t-tests within each group and condition separately. We found significant target preferences for the autistic group in both conditions (focused interest condition proportion of target looking = 0.57 (SD = 0.35); t(35) = 2.38, p = .023; neutral condition proportion of target looking = 0.60 (SD = 0.36): intercept t(37) = 2.74, p = .0093), but in the nonautistic group, target preference was only above chance in the neutral condition (proportion of target looking = 0.63 (SD = 0.33); t(37) = 2.43, p = .020), not in the focused interest condition (proportion of target looking = 0.53 (SD = 0.34); t(39) = −0.46, p = .65). This suggests that autistic children learned the novel words in both conditions, and nonautistic children only learned in the neutral condition.
Post-hoc Analyses Set #3.
Finally, the third set of post-hoc analyses included a detailed exploration of the timing of children’s responses during the Response period. This analysis was motivated by visual inspection of the data, which suggested that our pre-selected analysis window of 1 to 2.5 seconds of the Response Phase was too late, and that children were already showing a preference for the target at the beginning of this time window. Therefore, we pursued growth curve analyses of the period from 200–999 ms. For the autistic group, the best-fitting model included second-order (linear and quadratic) orthogonal polynomials, and it included a fixed effect of condition and random effect of participant with a random slope for the linear time term (the model failed to converge with a random slope for the quadratic time term). This model revealed a significant simple effect of condition (β = 0.35, t = 2.79, p = 0.0054) and significant interactions between condition and both time terms (interaction with linear term β = 1.22, t = 3.56, p =0.0004; interaction with quadratic time term β = −0.74, t = −2.25, p = 0.025), confirming that children’s gaze patterns differed between conditions before the analysis window began, as evident in Figure 2. The effect of condition indicates that autistic children looked to the target more in the focused interest condition overall, and that gaze in the focused interest condition increased over time, while it did not in the neutral condition.
For the nonautistic group, the best-fitting model for the period from 200–999 ms of the Response Phase included a first-order (linear) orthogonal polynomial, and it included a fixed effect of condition and random effect of participant with a random slope for the linear time term. This model revealed a significant simple effect of condition (β = 0.28, t = 2.27, p = 0.024) and a significant interaction between condition and the linear time term (β = −1.021, t = −2.92, p = 0.0037). The effect of condition indicates that nonautistic children looked to the target more in the focused interest condition overall, but that gaze in the focused interest condition remained flat over the time window while it increased linearly in the neutral condition.
In summary, taking the pre-registered and post-hoc analyses together, our findings indicate that autistic children showed evidence of increased looking toward the target in both conditions, but that they preferred the target earlier in the focused interest condition than in the neutral condition. Post-hoc comparisons to chance further highlight that the autistic children showed evidence of learning the words in both conditions. For the nonautistic children, our results indicate that they showed a stronger preference for the target in the neutral condition as compared to the focused interest condition, and that the difference between conditions began before and persisted through our pre-selected analysis window. Post-hoc comparisons to chance further highlight that only in the neutral condition was nonautistic children’s preference for the target scene sufficiently strong as to indicate learning.
DISCUSSION
Young children—autistic and nonautistic—commonly have focused interests in the preschool and early school age period. Following previous research pointing to the value of these interests for learning, we asked whether children’s focused interests could be harnessed for word learning. In contrast to a previous design which explored the teaching of new labels which were intrinsically related to the focused interest (e.g., learning names of vehicles for a child interested in vehicles, Ackerman et al., 2020), we asked whether learning is supported when the focused interest depicted a conceptually unrelated referent. We expected that, across groups, children would perform better when the task invoked their focused interest than when it was depicted by a neutral interest. Results did not align with our hypothesis but in different ways across the autistic and nonautistic groups.
In the autistic group, our pre-registered analysis indicated a difference between conditions in children’s attention to the target, with autistic children shifting to the target earlier in the interest condition than in the neutral condition. However, post-hoc analyses indicated that—for the autistic sample—children learned the new word (i.e., performed above chance) in both experimental conditions. The post-hoc analyses are also suggestive of a boost in the focused interest condition as reflected in an earlier preference for the target (even preceding our pre-registered analysis window); future work should pursue this possibility directly. In sum, on the one hand, children on the autism spectrum failed to show the expected learning advantage in the focused interest condition; on the other hand, they did exhibit—as hypothesized—successful word learning in the focused interest condition, and were possibly even faster to demonstrate this learning when their focused interest was present.
In the nonautistic group, the preregistered analysis revealed that the nonautistic group preferred the target more in the neutral condition than in the focused interest condition, and that this preference persisted over the course of the analysis window. Post-hoc analyses revealed a learning disadvantage when the task depicted their focused interest, such that the nonautistic sample learned the new word (i.e., performing above chance) only when the activity relied on a neutral image and not when it invoked their focused interest.
Although this study does not reveal the mechanism by which focused interests affect word learning, the literature offers several possibilities to consider. One set of previous findings points to the importance of visual salience in word learning and has yielded somewhat mixed findings across studies and across diagnostic groups. While Pomper and Saffran (2018) reported that the presence of highly salient familiar objects interrupted novel word learning for nonautistic preschoolers, Venker et al. (2022) reported that highly visually salient novel objects supported word learning for nonautistic preschoolers. In contrast, Venker et al. (2022) reported that autistic children failed to learn new words when novel objects were highly visually salient. In locating our findings within these previous reports, it is important to highlight a distinction between these previous studies and the present one: visual salience (as in these prior reports) versus conceptual salience (as in the present study). Here, we aimed to make conditions similar in important visual features (e.g., animacy and size) but different in their cognitive and preferential significance to the child (more on this below). We expect that this contrast might explain the differences observed between the present study and Venker et al. (2022). However, the present report is more similar to the Pomper and Saffran (2018) study, in which salient objects were familiar (not novel, as in Venker et al., 2022), and where the nonautistic children struggled to successfully map new words.
In making further sense of these findings, it is perhaps important to highlight some critical components of the experimental design used in the present study. First, at no point in the training trials was there more than one image on the screen. Second, at no point in the test trials was the neutral interest presented simultaneously as the focused interest. Moreover, the test trials present the same image completing different actions; therefore, within trials, the visual salience of the two images is well-matched (though they are completing slightly different movements on the screen). All of these design features reduce the likelihood that “sticky” visual attention (Sacrey et al., 2013; Bryson et al., 2018) is likely to provide a clear explanation for our findings (as in, for instance, Venker et al., 2022). Finally, it is important to note that the action presented was not thematically related to the interest; the character in the image enacted an action that was conceptually unrelated to the interest. In sum, it is important to differentiate visual attention from cognitive processing; that is, to distinguish the demands associated with shifting one’s eyes between an image and a different image versus the demands of shifting one’s thinking between an image and a different concept. Here, we turn to a second possible explanation for our study findings: focused interests may affect cognitive or attentional processing in different ways for autistic and nonautistic children.
A recent study with autistic and nonautistic adolescents and young adults in a personalized selective attention task found that for nonautistic individuals, items related to their interests yielded automatic top-down priority for attention over other objects; however, autistic individuals did not show this pattern (Parsons, Bayliss, Remington, 2017). There have been other reports that visual stimuli (especially those with personal salience, similar to the present study) can support higher-level cognitive tasks for nonautistic children, but only if the images are relevant to the mental task; visual images fail to facilitate these cognitive tasks if they are unrelated to the mental activity (Qu & Zelazo, 2007), as they are in the current study. In sum, for nonautistic children in our task, it could be that this automatic, mental prioritization of their interest perhaps diminished their ability to dedicate simultaneous cognitive resources to decipher the (unrelated) meaning of the novel word. This could indicate that nonautistic children’s cognitive processing is relatively susceptible to certain aspects of the stimuli, and that this might—under some circumstances—hinder performance by fracturing children’s focus.
In contrast, autistic children may have some differences in the way that they process and integrate the various task components demanding their attention (i.e., visual image of focused interest, auditory input presenting the new word). Many previous accounts have characterized attention and cognition in autism as very focused and persistent; some scholars have invoked the idea of “monotropism” to characterize attention in autism (Murray, 1992; Woods and Waltz, 2019). Murray and colleagues (2015) describe monotropism as follows:
Our hypothesis is that the difference between autistic and non-autistic is a difference in the strategies employed in the distribution of scarce attention. That is to say, it is the difference between having few interests highly aroused, the monotropic tendency, and having many interests less highly aroused, the polytropic tendency (p. 140).
The authors discuss how this highly focused attention style can be a detriment when individuals are asked to shift their attention to a task that they see as unmotivating or unrelated to a preferred interest. However, when autistic individuals perceive an activity as connected to their focus of attention, and therefore find that task motivating, this attention style may be advantageous: “If the understanding and the motivation are present, even the least evidently able people with autism may be able to do some things strikingly well” (Murray et al., 2005, p. 144), and that “there may be no problems in integrating information when it is attended to” (p. 141). Finally, the authors suggest that learning (or learning difficulties) may be related to the extent to which instruction has been motivated by personal interests: “We suggest that the uneven skills profile in autism depends on which interests have been fired into monotropic superdrive and which have been left unstimulated by any felt experience” (Murray et al., 2005, p. 143). Our results are broadly consistent with this characterization of attention in autism, particularly in the context of a focused interest.
Although we think that monotropism is an interesting explanation for our results and has support from the literature, it is important to note that another possible explanation for difference across groups in the focused interest condition is simply that the two groups differed in age (in order to allow for matching on vocabulary size). Younger children could struggle for the complex processing reason outlined above; in short, younger children have more difficulty in simultaneous cognitive processes. However, we note that the autistic and nonautistic groups overlapped substantially in age. Future researchers might consider whether using multiple comparison groups (i.e., one matched on language level and one matched on age, as well as matching on language measures other than vocabulary size) would enrich our understanding, given that the roles of cognitive processing, attention and focused interests may change over development independently of changes in language ability.
There are some additional important limitations of this work that are important to acknowledge. First, the developmental timing of focused interests is variable across studies, with some indicating that focused interests are established by the preschool years (Alexander et al., 2008; Burrows et al., 2021; DeLoache et al., 2007) and others suggesting an onset closer to age 5 (Nowell et al., 2021). If interests generally emerge closer to age 5, then a slightly older sample than the one we report here might be valuable. Finally, while remote testing in participants’ homes offers several advantages, there are challenges associated with measuring eye gaze in response to linguistic stimuli, such as differences in frame rate and differences in the devices that participants used. We did take several steps to mitigate these concerns as described above, and we note that many researchers have replicated findings of in-lab studies using remote procedures (e.g., Bacon, Weaver, & Saffran, 2021; Luyster et al., under revision; Scott, Chu, & Schulz, 2017).
Finally, in terms of testing word learning, there are a variety of features of our design that must be acknowledged so that future research might consider how performance might vary according to trial features. It is important to highlight that our study employed only one trial per condition (following, e.g., Yuan & Fisher, 2009), and some children did not contribute a useable trial to both conditions (note that our pattern of results did not substantively change when we included only children who contributed data across both conditions). The task also did not require extension of the newly learned word to a new agent—instead, both the target and distractor depicted either the same interest or neutral image as during the training phase; it also only required children to learn one novel label at a time, rather than the more stringent test of learning names for both the target and distractor (Axelsson & Horst, 2013). Additional studies that vary these design features would measure the robustness and generalizability of word learning. Moreover, although our analysis window was based on previous literature, future research could consider the effects of using different time windows (i.e., to avoid gaze shifts that may be less stimulus-driven).
There are a variety of valuable applied implications for the work reported here, the most important of which is that invoking a child’s focused interest did not appear to interfere with language learning; to the contrary, invoking a child’s focused interest resulted in successful word learning. While there was no apparent learning advantage for invoking children’s focused interests, there are associated and important “real world” benefits for doing so. First, for caregivers, providers and clinicians supporting young autistic children, our work aligns with the suggestions of Wood (2021): accepting children’s focused interests may be valuable in supporting child participation and communication. Second, it may have collateral benefits for caregivers and instructors, reducing the need for them to offer persistent prompts and direction (Wood, 2021). There are similar ramifications for naturalistic developmental behavioral interventions, in which “clinicians take advantage of a child’s existing interests and preferred activities as a means to maximize engagement, responsiveness, and skill acquisition” for infants and young children (italics added; Schuck et al., 2021) as well as for clinical programs more broadly (e.g., Harrop et al., 2019). In fact, explicit incorporation of focused interests is central to the design of some intervention protocols, such as “PowerCards” (Gagnon, 2001). Moreover, our work supports a conclusion drawn by another recent word learning study in autistic children highlighting the importance of using stimuli that “appealed to the strengths of children with ASD” (Hartley, Bird, & Monaghan, 2019). We hope that this study, in combination with these other recent advancements, will support the development of motivating, individualized and effective strategies for supporting language development in individuals on the autism spectrum.
Supplementary Material
Acknowledgements:
We would like to express our gratitude to Thuy Buonocore, Taylor Boyd, Estefanía Narvaez, and Urvisha Shethia for their help with data collection and coding; to Catherine Sancimino, Psy.D. for diagnostic confirmation; to Kristie Patten for helpful discussion about autistic interests; to our Autistic Advisory Board for their insights into the autistic experience; and to the anonymous reviewers who had exceptionally constructive comments. We would especially like to thank the many children and families who shared their time with us as part of this study, including all of the families at the participating Simons Simplex Collection (SSC) sites, as well as the principal investigators (A. Beaudet, R. Bernier, J. Constantino, E. Cook, E. Fombonne, D. Geschwind, R. Goin-Kochel, E. Hanson, D. Grice, A. Klin, D. Ledbetter, C. Lord, C. Martin, D. Martin, R. Maxim, J. Miles, O. Ousley, K. Pelphrey, B. Peterson, J. Piggot, C. Saulnier, M. State, W. Stone, J. Sutcliffe, C. Walsh, Z. Warren, E. Wijsman). We appreciate obtaining access to phenotypic data on SFARI Base. Approved researchers can obtain the SSC population dataset by applying at https://base.sfari.org.
Funding:
This work was supported by the National Institutes of Health (NIH R01DC017131) to SA and RL. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Footnotes
As indicated in our preregistration, we planned to exclude children who did not complete both trials, because we were concerned that children who “fussed out” of one of the trials might differ systematically from those who did not (e.g., children who were overstimulated if their focused interest was presented first and did not sit through the second trial). All participants did sit through and complete both trials. However, after removing individuals for parent report of child interest on the day of study and for track loss, only one trial remained in the final analyses for some participants. Following a reviewer suggestion, we repeated the analyses on only children who contributed both trials; the patterns were the same. These post-hoc analyses are available on OSF.
As part of our post-hoc analyses, we repeated the analyses on the full group of autistic participants, including those with very low language scores who could not be matched to a nonautistic participant. The patterns were the same, and showed that in both conditions, children with higher vocabularies showed a stronger preference for the target. The analyses are available on OSF.
Caregivers were also asked to complete the Survey of Favorite Interests and Activities (SOFIA; Smerbeck, 2017) to rate the child’s behavior relative to their focused interests on a scale of 1 (never or not at all true) to 5 (very frequently or totally true). These results capture children’s behavior and interests in general, not the specific interests used in the current study; consequently, these data were not used. We report on the SOFIA data elsewhere (Turner et al., in prep).
Because frame rates vary slightly when videos are played on different devices with different internet connectivity, etc., we coded the videos using audio cues within each trial; by “restarting” the coding from each audio cue, we ensured that any lag that accumulated over the course of playing a video was reset at each critical time point and did not persist over the course of the entire video. The longest time period over which lag could have accumulated using this procedure was 2.5 seconds; spot-checking of several videos indicated that they rarely differed in frame length over this short time period, and if they did it was only by 1–2 frames.
Following a reviewer suggestion, we repeated the analyses excluding frames on which children were looking to neither the target nor distractor. The patterns were identical except that for the nonautistic children, the interaction between time and condition was not significant (p = .099). We also repeated all post-hoc analyses with this dependent variable. The results are available on OSF.
Following a reviewer suggestion, we re-ran these analyses including a random slope for condition. These models did not converge.
Figures depicting the predicted slopes by condition for all models are available on OSF.
Conflicts of Interest: The authors have no conflicts of interest to report.
Data Availability Statement:
The data that support the findings of this study are openly available at https://osf.io/ra4un/.
REFERENCES
- Abu-Zhaya R, Goffman L, Brosseau-Lapré F, Roepke E, & Seidl A (2023). The Effect of Somatosensory Input on Word Recognition in Typical Children and Those With Speech Sound Disorder. Journal of Speech, Language, and Hearing Research, 1–14. 10.1044/2022_jslhr-22-00226 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ackermann L, Hepach R, & Mani N (2020). Children learn words easier when they are interested in the category to which the word belongs. Developmental Science, 23(3), 1–12. 10.1111/desc.12915 [DOI] [PubMed] [Google Scholar]
- Ackermann L, Förster M, Schaarschmidt J, Hepach R, Mani N, & Eiteljoerge S (2023). The role of interest in young children’s retention of words. Infant and Child Development, e2466. [Google Scholar]
- Alexander JM, Johnson KE, & Schreiber JB (2002). Knowledge is not everything: Analysis of children’s performance on a haptic comparison task. Journal of Experimental Child Psychology, 82(4), 341–366. 10.1016/s0022-0965(02)00100-5 [DOI] [PubMed] [Google Scholar]
- Alexander JM, Johnson KE, Leibham ME, & Kelley K (2008). The development of conceptual interests in young children. Cognitive Development, 23(2), 324–334. 10.1016/j.cogdev.2007.11.004 [DOI] [Google Scholar]
- Ambarchi Z, Boulton KA, Thapa R, Thomas EE, DeMayo MM, Sasson NJ, Hickie IB, & Guastella AJ (2022). Evidence of a reduced role for circumscribed interests in the social attention patterns of children with autism spectrum disorder. Journal of Autism and Developmental Disorders. 1–3. 10.1007/s10803-022-05638-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anthony LG, Kenworthy L, Yerys BE, Jankowski KF, James JD, Harms MB, Martin A, & Wallace GL (2013). Interests in high-functioning autism are more intense, interfering, and idiosyncratic than those in neurotypical development. Development and Psychopathology, 25(3), 643–652. 10.1017/s0954579413000072 [DOI] [PMC free article] [PubMed] [Google Scholar]
- American Psychiatric Association (APA). (2013). Diagnostic and statistical manual of mental disorders (5th ed.). Arlington, VA: Author. [Google Scholar]
- Arunachalam S, & Dennis S (2019). Semantic detail in the developing verb lexicon: An extension of Naigles and Kako (1993). Developmental Science, 22(1), 1–12. 10.1111/desc.12697 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Axelsson EL, & Horst JS (2013). Testing a word is not a test of word learning. Acta Psychologica, 144(2), 264–268. 10.1016/j.actpsy.2013.07.002 [DOI] [PubMed] [Google Scholar]
- Bacon D, Weaver H, & Saffran J (2021). A framework for online experimenter-moderated looking-time studies assessing infants’ linguistic knowledge. Frontiers in Psychology, 12, 703839. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bal VH, Kim S-H, Fok M, & Lord C (2018). Autism spectrum disorder symptoms from ages 2 to 19 years: Implications for diagnosing adolescents and young adults. Autism Research, 12(1), 89–99. 10.1002/aur.2004 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barr DJ (2008). Analyzing ‘visual world’ eyetracking data using multilevel logistic regression. Journal of Memory and Language, 59(4), 457–474. 10.1016/j.jml.2007.09.002 [DOI] [Google Scholar]
- Bates D, Mächler M, Bolker B, & Walker S (2015). Fitting linear mixed-effects models using lme4. Journal of Statistical Software, 67(1). 10.18637/jss.v067.i01 [DOI] [Google Scholar]
- Blomquist C, Newman RS, Huang YT, & Edwards J (2021). Children with cochlear implants use semantic prediction to facilitate spoken word recognition. Journal of Speech, Language, and Hearing Research, 64(5), 1636–1649. 10.1044/2021_JSLHR-20-00319 [DOI] [PubMed] [Google Scholar]
- Borovsky A, Ellis EM, Evans JL, & Elman JL (2016). Lexical leverage: Category knowledge boosts real-time novel word recognition in 2-year-olds. Developmental Science, 19(6), 918–932. 10.1111/desc.12343 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bottema-Beutel K, Kapp SK, Lester JN, Sasson NJ, & Hand BN (2021). Avoiding ableist language: Suggestions for autism researchers. Autism in Adulthood. 10.1089/aut.2020.0014 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boyd BA, Conroy MA, Mancil GR, Nakao T, & Alter PJ (2007), Effects of circumscribed interests on the social behaviors of children with autism spectrrum disorders. Journal of Autism and Developmental Disorders, 37, 1550–1561. 10.1007/s10803-006-0286-8 [DOI] [PubMed] [Google Scholar]
- Brian J, Zwaigenbaum L, & Ip A (2019). Standards of diagnostic assessment for autism spectrum disorder. Paediatrics & Child Health, 24(7), 444–451. 10.1093/pch/pxz117 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bryson S, Garon N, McMullen T, Brian J, Zwaigenbaum L, Armstrong V, Roberts W, Smith I, & Szatmari P (2018). Impaired disengagement of attention and its relationship to emotional distress in infants at high-risk for autism spectrum disorder. Journal of Clinical and Experimental Neuropsychology, 40(5), 487–501. 10.1080/13803395.2017.1372368 [DOI] [PubMed] [Google Scholar]
- Burrows CA, Bodfish JW, Wolff JJ, Vollman EP, Altschuler MR, Botteron KN, Dager SR, Estes AM, Hazlett HC, Pruett JR, Schultz RT, Zwaigenbaum L, Piven J, & Elison JT (2021). Cataloguing and characterizing interests in typically developing toddlers and toddlers who develop asd. Autism Research, 14(8), 1710–1723. 10.1002/aur.2543 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Carter RMK, Jung H, Reaven J, Blakeley-Smith A, & Dichter GS (2020). A Nexus model of restricted interests in autism spectrum disorder. Frontiers in Human Neuroscience, 14. 10.3389/fnhum.2020.00212 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Charman T, Drew A, Baird C, & Baird G (2003). Measuring early language development in preschool children with autism spectrum disorder using the MacArthur Communicative Development Inventory (Infant Form). Journal of Child Language, 30(1), 213–236. 10.1017/s0305000902005482 [DOI] [PubMed] [Google Scholar]
- Chawarska K, Klin A, & Volkmar F (2003). Automatic attention cueing through eye movement in 2-year-old children with autism. Child Development, 74(4), 1108–1122. 10.1111/1467-8624.00595 [DOI] [PubMed] [Google Scholar]
- Chiodo L, Majerus S, & Mottron L (2017). Typical versus delayed speech onset influences verbal reporting of autistic interests. Molecular Autism, 8(1), 1–12. 10.1186/s13229-017-0155-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Corsello C, Hus V, Pickles A, Risi S, Cook EH, Leventhal BL, & Lord C (2007). Between a ROC and a hard place: Decision making and making decisions about using the SCQ. Journal of Child Psychology and Psychiatry, 48(9), 932–940. 10.1111/j.1469-7610.2007.01762.x [DOI] [PubMed] [Google Scholar]
- Dautriche I, Cristia A, Brusini P, Yuan S, Fisher C, & Christophe A (2014). Toddlers default to canonical surface-to-meaning mapping when learning verbs. Child Development, 85(3), 1168–1180. 10.1111/cdev.12164 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Delle Luche C, Durrant S, Poltrock S, & Floccia C (2015). A methodological investigation of the Intermodal Preferential Looking paradigm: Methods of analyses, picture selection and data rejection criteria. Infant Behavior and Development, 40, 151–172. 10.1016/j.infbeh.2015.05.005 [DOI] [PubMed] [Google Scholar]
- DeLoache JS, Simcock G, & Macari S (2007). Planes, trains, automobiles--and tea sets: Extremely intense interests in very young children. Developmental Psychology, 43(6), 1579–1586. 10.1037/0012-1649.43.6.1579 [DOI] [PubMed] [Google Scholar]
- Dunst CJ, & Hamby DW (2016). Review of Single Participant Studies Investigating the Relationship Between the Interests and Social-Communication Behavior of Young Children with Autism Spectrum Disorders. Austin Journal of Autism & Related Disabilities. 2 (3), 1–7. [Google Scholar]
- Feliciano P, Daniels AM, Snyder LG, Beaumont A, Camba A, Esler A, ... & Brewster SJ (2018). SPARK: a US cohort of 50,000 families to accelerate autism research. Neuron, 97(3), 488–493. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fenson L, Marchman VA, Thal DJ, Dale PS, Reznick JS, & Bates E (2006). MacArthur-Bates Communicative Development Inventories, Second edition. PsycTESTS Dataset. 10.1037/t11538-000 [DOI] [Google Scholar]
- Fernald A, McRoberts GW, & Swingley D (2001). Infants’ developing competence in recognizing and understanding words in fluent speech. Language Acquisition and Language Disorders, 23, 97–124. [Google Scholar]
- Forbes S, Dink J, Ferguson B (2021). _eyetrackingR_. R package version## 0.2.0, <URL: http://www.eyetracking-r.com/>.
- Gagnon E (2001). Power cards: Using special interests to motivate children and youth with asperger syndrome and autism. Autism Asperger Publishing. [Google Scholar]
- Gamer M, & Lemon J (2019). _irr: Various Coefficients of Interrater Reliability and Agreement_. R package. <https://CRAN.R-project.org/package=irr>. [Google Scholar]
- Golinkoff RM, Hirsh-Pasek K, Cauley KM, & Gordon L (1987). The eyes have it: Lexical and syntactic comprehension in a new paradigm. Journal of Child Language, 14(1), 23–45. 10.1017/S030500090001271X [DOI] [PubMed] [Google Scholar]
- Grove R, Hoekstra RA, Wierda M, & Begeer S (2018). Special interests and subjective wellbeing in autistic adults. Autism Research, 11(5), 766–775. 10.1002/aur.1931 [DOI] [PubMed] [Google Scholar]
- Gunn KC, & Delafield-Butt JT (2016). Teaching children with autism spectrum disorder with restricted interests. Review of Educational Research, 86(2), 408–430. 10.3102/0034654315604027 [DOI] [Google Scholar]
- Hahn N, Snedeker J, & Rabagliati H (2015). Rapid linguistic ambiguity resolution in young children with autism spectrum disorder: Eye tracking evidence for the limits of weak central coherence. Autism Research, 8(6), 717–726. 10.1002/aur.1487 [DOI] [PubMed] [Google Scholar]
- Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, & Conde JG (2009). A metadata-driven methodology and workflow process for providing translational research informatics support. Journal of Biomedical Informatics, 42(2), 377–81. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harris PA, Taylor R, Minor BL, Elliott V, Fernandez M, O’Neal L, ... & REDCap Consortium. (2019). The REDCap consortium: building an international community of software platform partners. Journal of Biomedical Informatics, 95, 103208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harrop C, Amsbary J, Towner-Wright S, Reichow B, & Boyd BA (2019). That’s what I like: The use of circumscribed interests within interventions for individuals with autism spectrum disorder. A systematic review. Research in Autism Spectrum Disorders, 57, 63–86. 10.1016/j.rasd.2018.09.008 [DOI] [Google Scholar]
- Hartley C, Bird L-A, & Monaghan P (2019). Investigating the relationship between fast mapping, retention, and generalisation of words in children with autism spectrum disorder and typical development. Cognition, 187, 126–138. 10.1016/j.cognition.2019.03.001 [DOI] [PubMed] [Google Scholar]
- He AX, & Lidz J (2017). Verb learning in 14-and 18-month-old English-learning infants. Language Learning and Development, 13(3), 335–356. 10.1080/15475441.2017.1285238 [DOI] [Google Scholar]
- Hidi S (1990). Interest and its contribution as a mental resource for learning. Review of Educational Research, 60(4), 549–571. 10.3102/00346543060004549 [DOI] [Google Scholar]
- Horvath S, McDermott E, Reilly K, & Arunachalam S (2018). Acquisition of verb meaning from syntactic distribution in preschoolers with autism spectrum disorder. Language, Speech, and Hearing Services in Schools, 49(3S), 668–680. 10.1044/2018_lshss-stlt1-17-0126 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacques C, Courchesne V, Meilleur A-AS, Mineau S, Ferguson S, Cousineau D, Labbe A, Dawson M, & Mottron L (2018). What interests young autistic children? an exploratory study of object exploration and repetitive behavior. PLOS ONE, 13(12). 10.1371/journal.pone.0209251 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson KE, Alexander JM, Spencer S, Leibham ME, & Neitzel C (2004). Factors associated with the early emergence of intense interests within conceptual domains. Cognitive Development, 19(3), 325–343. 10.1016/j.cogdev.2004.03.001 [DOI] [Google Scholar]
- Johnson VE, & de Villiers JG (2009). Syntactic frames in fast mapping verbs: effect of age, dialect, and clinical status. Journal of Speech, Language, and Hearing Research: JSLHR, 52(3), 610–622. 10.1044/1092-4388(2008/07-0135) [DOI] [PubMed] [Google Scholar]
- Johnson KE, & Eilers AT (1998). Effects of knowledge and development on subordinate level categorization. Cognitive Development, 13(4), 515–545. 10.1016/s0885-2014(98)90005-3 [DOI] [Google Scholar]
- Klin A, Danovitch JH, Merz AB, & Volkmar FR (2007). Circumscribed interests in higher functioning individuals with autism spectrum disorders: An exploratory study. Research and Practice for Persons with Severe Disabilities, 32(2), 89–100. 10.2511/rpsd.32.2.89 [DOI] [Google Scholar]
- Kover ST, & Atwood AK (2013). Establishing equivalence: Methodological progress in group-matching design and analysis. American Journal on Intellectual and Developmental Disabilities, 118(1), 3–15. 10.1352/1944-7558-118.1.3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuznetsova A, Brockhoff PB, & Christensen RH (2017). lmertest package: Tests in linear mixed effects models. Journal of Statistical Software, 82(13). 10.18637/jss.v082.i13 [DOI] [Google Scholar]
- Larose V, Sotelo K, Mottron L, & Jacques C (2021). Initial development of a questionnaire about parents’ perspectives on the strengths and interests of autistic preschoolers. Canadian Journal of Behavioural Science / Revue Canadienne Des Sciences Du Comportement, 53(4), 530–535. 10.1037/cbs0000268 [DOI] [Google Scholar]
- Lenth R (2022). emmeans: estimated marginal means, aka least-squares means. R package version 1.4. 7. 2020. [Google Scholar]
- Luyster R, Boyd T, Steele A, & Arunachalam S (under revision). Quality of remotely-collected gaze data in autistic and non-spectrum children. [DOI] [PMC free article] [PubMed]
- Luyster R, Lopez K, & Lord C (2007). Characterizing communicative development in children referred for autism spectrum disorders using the MacArthur-Bates Communicative Development Inventory (CDI). Journal of Child Language, 34(3), 623–654. 10.1017/s0305000907008094 [DOI] [PubMed] [Google Scholar]
- Ma W, Luo R, Golinkoff R, & Hirsh-Pasek K (2023). The influence of exemplar variability on young children’s construal of verb meaning. Language Learning and Development, 1–26. 10.1080/15475441.2022.2060834 [DOI] [Google Scholar]
- Mahr T (2023). _bootmatch: Bootstrap Group Matching_. R package version 0.0.0.9000. [Google Scholar]
- Mani N, & Ackermann L (2018). Why do children learn the words they do? Child Development Perspectives, 12(4), 253–257. 10.1111/cdep.12295 [DOI] [Google Scholar]
- Mirman D (2014). Growth Curve Analysis and Visualization Using R. Chapman and Hall / CRC. [Google Scholar]
- Murray DKC (1992) ‘Attention Tunnelling and Autism’, in Living with Autism: The Individual, the Family, and the Professional Originally presented at the Durham Conference, UK. Proceedings obtainable from Autism Research Unit, School of Health Sciences,University of Sunderland, Sunderland SR2 7EE, UK. [Google Scholar]
- Murray D, Lesser M, & Lawson W (2005). Attention, monotropism and the diagnostic criteria for autism. Autism, 9(2), 139–156. 10.1177/1362361305051398 [DOI] [PubMed] [Google Scholar]
- Naigles LR, Kelty E, Jaffery R, & Fein D (2011). Abstractness and continuity in the syntactic development of young children with autism. Autism Research, 4(6), 422–437. 10.1002/aur.223 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Naigles LR, & Tovar AT (2012). Portable intermodal preferential looking (IPL): Investigating language comprehension in typically developing toddlers and young children with autism. JoVE (Journal of Visualized Experiments), (70), e4331. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ninci J, Neely LC, Burke MD, Rispoli M, Vannest KJ, Willson V, & Ulloa P (2019). A meta-analysis of single-case research on embedding interests of individuals with autism spectrum disorder. Remedial and Special Education, 41(5), 296–308. 10.1177/0741932519841692 [DOI] [Google Scholar]
- Nitzan T, Koller J, Ilan M, Faroy M, Michaelovski A, Menashe I, Meiri G, & Dinstein I (2022). The importance of language delays as an early indicator of subsequent ASD diagnosis in public healthcare settings. Journal of Autism and Developmental Disorders. 10.1007/s10803-022-05757-y [DOI] [PubMed] [Google Scholar]
- Nowell KP, Bernardin CJ, Brown C, & Kanne S (2021). Characterization of special interests in autism spectrum disorder: A brief review and pilot study using the Special Interests Survey. Journal of Autism and Developmental Disorders, 51(8), 2711–2724. 10.1007/s10803-020-04743-6 [DOI] [PubMed] [Google Scholar]
- Ostrolenk A, Courchesne V, & Motton L (2023). A longitudinal study on language acquisition in monozygotic twins concordant for autism and hyperlexia. Brain and Cognition, 173, 106099. 10.1016/j.bandc.2023.106099 [DOI] [PubMed] [Google Scholar]
- Parsons OE, Bayliss AP, & Remington A (2017). A few of my favorite things: Circumscribed interests in autism are not accompanied by increased attentional salience on a personalized selective attention task. Molecular Autism, 8(1). 10.1186/s13229-017-0132-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Patten Koenig K, & Hough Williams L (2017). Characterization and utilization of preferred interests: A survey of adults on the autism spectrum. Occupational Therapy in Mental Health, 33(2), 129–140. 10.1080/0164212x.2016.1248877 [DOI] [Google Scholar]
- Pelletier T, & Arunachalam S (2021). Do preferred interests support vocabulary learning in preschoolers with ASD? A pilot study. Poster presented at the International Society for Autism Research (INSAR). [Google Scholar]
- Pickles A, Anderson DK, & Lord C (2014). Heterogeneity and plasticity in the development of language: A 17-year follow-up of children referred early for possible autism. Journal of Child Psychology and Psychiatry, 55(12), 1354–1362. 10.1111/jcpp.12269 [DOI] [PubMed] [Google Scholar]
- Pomper R, & Saffran JR (2018). Familiar object salience affects novel word learning. Child Development, 90(2). 10.1111/cdev.13053 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qu L, & Zelazo PD (2007). The facilitative effect of positive stimuli on 3-year-olds’ flexible rule use. Cognitive Development, 22(4), 456–473. 10.1016/j.cogdev.2007.08.010 [DOI] [Google Scholar]
- Renninger KA (1992). Individual interest and development: Implications for theory and practice. In Renninger KA, Hidi S, & Krapp A (Eds.), The role of interest in learning and development (pp. 361–395). Hillsdale, NJ: Erlbaum. 10.4324/9781315807430-10 [DOI] [Google Scholar]
- Renninger KA, & Wozniak RH (1985). Effect of interest on attentional shift, recognition, and recall in young children. Developmental Psychology, 21(4), 624–632. 10.1037/0012-1649.21.4.624 [DOI] [Google Scholar]
- Rothwell C, Westermann G, & Hartley C (2023). How do autistic and neurotypical children’s interests influence their accuracy during novel word learning? Journal of Autism and Developmental Disorders. 10.1007/s10803-023-06066-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rutter M, Bailey A, & Lord C (2003). SCQ. The Social Communication Questionnaire. Torrance, CA: Western Psychological Services. [Google Scholar]
- Sacrey L-AR, Bryson SE, & Zwaigenbaum L (2013). Prospective examination of visual attention during play in infants at high-risk for autism spectrum disorder: A longitudinal study from 6 to 36 months of age. Behavioural Brain Research, 256, 441–450. 10.1016/j.bbr.2013.08.028 [DOI] [PubMed] [Google Scholar]
- Sasson NJ, & Touchstone EW (2013). Visual attention to competing social and object images by preschool children with autism spectrum disorder. Journal of Autism and Developmental Disorders, 44(3), 584–592. 10.1007/s10803-013-1910-z [DOI] [PubMed] [Google Scholar]
- Sasson NJ, Elison JT, Turner-Brown LM, Dichter GS, & Bodfish JW (2011). Brief report: Circumscribed attention in young children with autism. Journal of Autism and Developmental Disorders, 41(2), 242–247. 10.1007/s10803-010-1038-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schuck RK, Tagavi DM, Baiden KM, Dwyer P, Williams ZJ, Osuna A, Ferguson EF, Jimenez Muñoz M, Poyser SK, Johnson JF, & Vernon TW (2021). Neurodiversity and autism intervention: Reconciling perspectives through a naturalistic developmental behavioral intervention framework. Journal of Autism and Developmental Disorders, 52(10), 4625–4645. 10.1007/s10803-021-05316-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scott K, Chu J, & Schulz L (2017). Lookit (Part 2): Assessing the viability of online developmental research, results from three case studies. Open Mind, 1(1), 15–29. 10.1162/opmi_a_00001 [DOI] [Google Scholar]
- Sivaraman M, & Fahmie TA (2018). Using common interests to increase socialization between children with autism and their peers. Research in Autism Spectrum Disorders, 51, 1–8. 10.1016/j.rasd.2018.03.007 [DOI] [Google Scholar]
- Smerbeck A (2017). The Survey of Favorite Interests and Activities: Assessing and understanding restricted interests in children with autism spectrum disorder. Autism, 23(1), 247–259. 10.1177/1362361317742140 [DOI] [PubMed] [Google Scholar]
- Sparrow SS, Cicchetti DV & Saulnier CA (2016) Vineland Adaptive Behavior Scales, Third edn. San Antonio, TX, Pearson. [Google Scholar]
- Spiker MA, Lin CE, Van Dyke M, & Wood JJ (2011). Restricted interests and anxiety in children with autism. Autism, 16(3), 306–320. 10.1177/1362361311401763 [DOI] [PubMed] [Google Scholar]
- Tager-Flusberg H (2016). Risk factors associated with language in autism spectrum disorder: Clues to underlying mechanisms. Journal of Speech, Language, and Hearing Research, 59(1), 143–154. 10.1044/2015_jslhr-l-15-0146 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tager-Flusberg H, & Kasari C (2013). Minimally Verbal School-aged children with autism spectrum disorder: The neglected end of the spectrum. Autism Research, 6(6), 468–478. 10.1002/aur.1329 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Turner R, Luyster RJ, & Arunachalam S (in prep). Focused interests in autistic and non-autistic preschoolers: Data from the Survey of Favorite Interests and Activities. [Google Scholar]
- Venker CE, Neumann D, & Aladé F (2022). Visual perceptual salience and novel referent selection in children with and without autism spectrum disorder. Autism & Developmental Language Impairments, 7, 23969415221085476. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Verdine BN, Bunger A, Athanasopoulou A, Golinkoff RM, & Hirsh-Pasek K (2017). Shape up: An eye-tracking study of preschoolers’ shape name processing and spatial development. Developmental Psychology, 53(10), 1869. 10.1037/dev0000384 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vismara LA, & Lyons GL (2007). Using perseverative interests to elicit joint attention behaviors in young children with autism. Journal of Positive Behavior Interventions, 9(4), 214–228. 10.1177/10983007070090040401 [DOI] [Google Scholar]
- Wickham H (2016). Package ‘ggplot2’: elegant graphics for data analysis. Springer-Verlag New York. doi, 10, 978–0. [Google Scholar]
- Winter-Messiers MA (2007). From tarantulas to toilet brushes. Remedial and Special Education, 28(3), 140–152. 10.1177/07419325070280030301 [DOI] [Google Scholar]
- Wood R (2021). Autism, intense interests and support in school: From wasted efforts to shared understandings. Educational Review, 73(1), 34–54. [Google Scholar]
- Woods R, & Waltz M (2019). The strength of autistic expertise and its implications for autism knowledge production: A response to Damian Milton. Autonomy, the Critical Journal of Interdisciplinary Autism Studies, 1(6). [Google Scholar]
- Yuan S, & Fisher C (2009). “Really? She blicked the baby?” Two-year-olds learn combinatorial facts about verbs by listening. Psychological Science, 20(5), 619–626. 10.1111/j.1467-9280.2009.02341.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zwaigenbaum L & Penner M (2018). Autism spectrum disorder: advances in diagnosis and evaluation. BMJ: British Medical Journal, 361, 1–16. 10.1136/bmj.k1674 [DOI] [PubMed] [Google Scholar]
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This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The data that support the findings of this study are openly available at https://osf.io/ra4un/.
